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1. Safety Pharmacology in Pharmaceutical Development

   Approval and Post Marketing Surveillance, Second Edition

   By Shayne C. Gad

   This book covers the regulatory required evaluation and study of the potentially adverse pharmacological effects of new drugs. Coverage ranges from the general regulatory requirements to the specific studies that must be done and how they are performed and interpreted. Based on more than 30 years...

   Published April 25th 2012 by CRC Press
2. Safety Pharmacology in Pharmaceutical Development and Approval

   By Shayne C. Gad, Shayne C. Gad

   The Propulsid and Seldane drug disasters could have easily been avoided with more rigorous safety pharmacology studies of these compounds prior to any human clinical trials. Unfortunately, safety pharmacology has been overlooked by all but a few developers. With recent drug withdrawals from the...

   Published August 25th 2003 by CRC Press
3. The Selection and Use of Contract Research Organizations

   By Shayne C. Gad

   Choosing the right contract research organization (CRO) can make the difference between getting a product to market quickly and cost-effectively, and wasting valuable time and money. The vast number of available CROs is increasing all the time, and all of them make impressive claims. The Selection...

   Published July 2nd 2003 by CRC Press
4. Handbook of Data Recording, Maintenance, and Management for the Biomedical Sciences

   By Shayne C. Gad, Stephanie M. Taulbee

   The Handbook of Data Recording, Maintenance, and Management for the Biomedical Sciences explains how to maintain a scientific log that will withstand peer, federal, and other reviewing agencies' scrutiny. This is a timely publication as the maintenance of a log becomes an increasingly more...

   Published July 7th 1996 by CRC Press